Variant report

Variant rs10124464
Chromosome Location chr9:79039091-79039092
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:79034800-79046000 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr9:79036800-79039200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
3 chr9:79037400-79039400 Enhancers Primary T helper memory cells from peripheral blood 1 blood
4 chr9:79038000-79046800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr9:79038200-79039400 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:79038200-79039600 Enhancers Primary T cells from cord blood blood
7 chr9:79038200-79039800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr9:79038400-79039600 Enhancers Primary T helper cells fromperipheralblood blood
9 chr9:79038600-79039400 Enhancers Primary T helper naive cells from peripheral blood blood
10 chr9:79038800-79039400 Enhancers Stomach Mucosa stomach
11 chr9:79039000-79039400 Enhancers Primary T helper cells PMA-I stimulated --
12 chr9:79039000-79039400 Flanking Active TSS HepG2 liver

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